Disease #01596 (CMH1 (cardiomyopathy, hypertrophic, familial, type 1 (CMH-1)), OMIM:192600)

Official abbreviation CMH1
Name cardiomyopathy, hypertrophic, familial, type 1 (CMH-1)
OMIM ID 192600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Digenic dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 4 genes CAV3, MYH6, MYH7, MYLK2
Associated tissues -
Disease features -
Remarks -

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